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Adaptation to Brassica Host Genotypes by a Single-Spore Isolate and Population of Plasmodiophora brassicae (Clubroot)

June 2012 , Volume 96 , Number  6
Pages  833 - 838

J. M. LeBoldus, Department of Plant Pathology, North Dakota State University, Fargo, ND 58108, USA; V. P. Manolii, Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2P5, Canada; T. K. Turkington, Lacombe Research Centre, Agriculture and Agri-Food Canada, Lacombe, AB T4L 1W1, Canada; and S. E. Strelkov, Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton, AB T6G 2P5, Canada



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Accepted for publication 15 December 2011.
Abstract

Plasmodiophora brassicae, the cause of clubroot of crucifers, is an increasingly important pathogen of canola (Brassica napus) in Alberta, Canada. In response, clubroot-resistant canola genotypes are being deployed to help reduce yield losses. Two experiments were conducted to examine the effect on P. brassicae virulence of repeated exposure of a population and single-spore isolate of the pathogen to the same host. The first experiment examined changes in the index of disease over five cycles of infection on seven Brassica hosts (European Clubroot Differential [ECD] 02, ECD 04, ECD 05, ECD 15, ‘45H26’, ‘45H29’, and 08N823R). The second experiment tested the virulence of five cycled populations (‘45H29’, 08N823R, ECD 05, and ECD 15) and three cycled single-spore isolates (‘45H29’, 08N823R, and ECD05) on four resistant canola genotypes (‘73-77’, ‘73-67’, VT-SD-09, and ‘9558C’). The results from these experiments clearly demonstrate the ability of both single-spore isolates and populations of P. brassicae to rapidly erode the resistance present in the two canola genotypes, ‘45H29’ and 08N823R. Although the index of disease increased on these two genotypes, the four resistant canola genotypes remained resistant to all the cycled populations and single-spore isolates in the second experiment. These results underscore the importance of crop rotation in the management of clubroot in Alberta.



© 2012 The American Phytopathological Society